Fenofibrate Combined With Ursodeoxycholic Acid in Subjects With Primary Biliary Cholangitis

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18-75
SponsorXijing Hospital of Digestive Diseases

About this trial

Current treatment guidelines recommend ursodeoxycholic acid (UDCA) as the first-line treatment for new-diagnosed primary biliary cholangitis (PBC) patients. However, up to 40% patients are insensitive to UDCA monotherapy, and evaluation of UDCA response at 12 months may result in long period of ineffective treatment. We aimed to develop a new criterion to reliably identify non-response patients much earlier. Recently, our team designed and validated a new early criterion for distinguishing high-risk PBC patients in a Chinese population for the first time. Our data indicated that PBC patients with ALP ≤ 2.5 × ULN, AST ≤ 2 × ULN, and TBIL ≤ 1 × ULN (Xi'an criterion) after 1 month UDCA treatment were likely to have better prognosis. It can be readily applied in the rapid identification of PBC patients who require additional therapeutic approaches. However, whether it is reasonable to apply it to the response definition of clinical research, and the guidance of PBC management and choice of second-line treatment, further research is needed.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Must have provided written informed consent;

Age 18-75 years;

BMI 17-28 kg/m2

History of AP above ULN for at least six months;

Disqualifiers

History or presence of other concomitant liver diseases.

ALT/AST > 5×ULN, TBIL > 3×ULN.

If female: known pregnancy, or has a positive urine pregnancy test (confirmed by a positive serum pregnancy test), or lactating.

Allergic to fenofibrate or ursodeoxycholic acid.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Placebo Combined With Ursodeoxycholic Acid

    Drug

    1 tablet/ day

  • Fenofibrate Combined With Ursodeoxycholic Acid

    Drug

    200 mg/day

Treatment groups

150 Participants
are divided into 2 treatment groups
Group A: PlaceboPlacebo comparator 1 intervention
Group B: FenofibrateExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Percentage of patients with complete biochemical response

The normalisation of Alkaline Phosphatase (ALP) and total bilirubin (TBIL).

Time frame
48 weeks

Secondary outcomes

1

Percentage of patients having complete biochemical response

The normalisation of Alkaline Phosphatase (ALP) and total bilirubin (TBIL) at 4, 12, 24, and 36 weeks.

Time frame
4, 12, 24, 36, and 48 weeks
2

Assessment of the fatigue and the quality of life

Change from baseline in primary biliary cholangitis -40 (PBC-40) quality of life (QoL) questionnaire scores.

Time frame
4, 12, 24, 36, and 48 weeks
3

Assessment of the fatigue and the quality of life

Change from baseline in pruritus as assessed by Visual Analogue Scale (VAS) total score for fatigue and pruritus.

Time frame
4, 12, 24, 36, and 48 weeks
4

Evolution of the biological markers of the hepatic function or being in the usual prognostic scores

Mayo score at 4, 12, 24, 36, and 48 weeks

Time frame
4, 12, 24, 36, and 48 weeks

Other outcomes

Sponsors and contacts

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